Explore the words cloud of the AlCat project. It provides you a very rough idea of what is the project "AlCat" about.
The following table provides information about the project.
Coordinator |
THE UNIVERSITY OF EDINBURGH
Organization address contact info |
Coordinator Country | United Kingdom [UK] |
Total cost | 1˙493˙679 € |
EC max contribution | 1˙493˙679 € (100%) |
Programme |
1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC)) |
Code Call | ERC-2016-STG |
Funding Scheme | ERC-STG |
Starting year | 2017 |
Duration (year-month-day) | from 2017-03-01 to 2022-02-28 |
Take a look of project's partnership.
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1 | THE UNIVERSITY OF EDINBURGH | UK (EDINBURGH) | coordinator | 1˙493˙679.00 |
This project will develop the principles required to enable bond-modifying redox catalysis based on aluminium by preparing and studying new Al(I) compounds capable of reversible oxidative addition.
Catalytic processes are involved in the synthesis of 75 % of all industrially produced chemicals, but most catalysts involved are based on precious metals such as rhodium, palladium or platinum. These metals are expensive and their supply limited and unstable; there is a significant need to develop the chemistry of non-precious metals as alternatives. On toxicity and abundance alone, aluminium is an attractive candidate. Furthermore, recent work, including in our group, has demonstrated that Al(I) compounds can perform a key step in catalytic cycles - the oxidative addition of E-H bonds.
In order to realise the significant potential of Al(I) for transition-metal style catalysis we urgently need to: - establish the principles governing oxidative addition and reductive elimination reactivity in aluminium systems. - know how the reactivity of Al(I) compounds can be controlled by varying properties of ligand frameworks. - understand the onward reactivity of oxidative addition products of Al(I) to enable applications in catalysis. In this project we will:
- Study mechanisms of oxidative addition and reductive elimination of a range of synthetically relevant bonds at Al(I) centres, establishing the principles governing this fundamental reactivity. - Develop new ligand frameworks to support of Al(I) centres and evaluate the effect of the ligand on oxidative addition/reductive elimination at Al centres. - Investigate methods for Al-mediated functionalisation of organic compounds by exploring the reactivity of E-H oxidative addition products with unsaturated organic compounds.
year | authors and title | journal | last update |
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2018 |
Stephanie J. Urwin, Gary S. Nichol, Michael J. Cowley Aluminium-mediated carbon–carbon coupling of an isonitrile published pages: 378-380, ISSN: 1359-7345, DOI: 10.1039/c7cc08415c |
Chemical Communications 54/4 | 2020-01-24 |
2018 |
Alessandro Bismuto, Michael J. Cowley, Stephen P. Thomas Aluminum-Catalyzed Hydroboration of Alkenes published pages: 2001-2005, ISSN: 2155-5435, DOI: 10.1021/acscatal.7b04279 |
ACS Catalysis 8/3 | 2020-01-24 |
2019 |
Rosalyn L. Falconer, Gary S. Nichol, Michael J. Cowley Flexible Coordination of N,P-Donor Ligands in Aluminum Dimethyl and Dihydride Complexes published pages: , ISSN: 0020-1669, DOI: 10.1021/acs.inorgchem.9b01061 |
Inorganic Chemistry | 2020-01-24 |
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